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US07989182B2 Nucleic acid encoding SCN1A variant 有权
编码SCN1A变体的核酸

Nucleic acid encoding SCN1A variant
Abstract:
A method of identifying a subject predisposed to a disorder associated with ion channel dysfunction, comprising ascertaining whether at least one of the genes encoding ion channel subunits in said subject has undergone a mutation event such that a cDNA derived from said subject has the sequence set forth in one of SEQ ID NOS: 1-134.
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